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HRID 240271作成日:2026年10月24日
(3R)-3-Aminopiperidine, 3-BOC protected → (R)-tert-butyl 1-(4-(2-cyanobenzyl)-6-methyl-5-oxo-4,5-dihydro-1,2,4-triazin-3-yl)piperidin-3-ylcarbamate
https://huagongshe.com/ja/reaction/240271
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | (3R)-3-Aminopiperidine, 3-BOC protected | HCID 1514172 | — |
| 反応物 | 2-((6-methyl-3-(methylthio)-5-oxo-1,2,4-triazin-4(5H)-yl)methyl)benzonitrile | HCID 58328534 | — |
| 生成物 | (R)-tert-butyl 1-(4-(2-cyanobenzyl)-6-methyl-5-oxo-4,5-dihydro-1,2,4-triazin-3-yl)piperidin-3-ylcarbamate | HCID 58328532 | — |
反応手順
The mixture of 2-((6-methyl-3-(methylthio)-5-oxo-1,2,4-triazin-4(5H)-yl)methyl)benzonitrile (6, 68 mg, 0.25 mmol) and (R)-tert-butyl piperidin-3-ylcarbamate (60 mg, 0.30 mmol) was ground for 5 min and then heated in a tube under nitrogen atmosphere at 130° C. for 13 h. The mixture was separated by silica gel column, and eluted with 2:1 to 1:1 petroleum ether-ethyl acetate and then with 1:1:2 petroleum ether-dichloromethane-ethyl acetate to give (R)-tert-butyl 1-(4-(2-cyanobenzyl)-6-methyl-5-oxo-4,5-dihydro-1,2,4-triazin-3-yl)piperidin-3-ylcarbamate (7). MS: m/z, 425 (100%, M+1), 447(40%, M+23).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08648073B2 |
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| 出典データセット | uspto-grants-2014_02 |
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| ORD ID | ord-aabb22075e924630b76bc00c261e1e7b |
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| 出典メモ | uspto-grants-2014_02 |
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